Transcriptome-based molecular subtypes and differentiation hierarchies improve the classification framework of acute myeloid leukemia

Author:

Cheng Wen-Yan1,Li Jian-Feng12ORCID,Zhu Yong-Mei1,Lin Xiang-Jie34ORCID,Wen Li-Jun56,Zhang Fan1,Zhang Yu-Liang1,Zhao Ming1,Fang Hai1,Wang Sheng-Yue1,Lin Xiao-Jing1,Qiao Niu1,Yin Wei1,Zhang Jia-Nan1,Dai Yu-Ting1ORCID,Jiang Lu1,Sun Xiao-Jian1ORCID,Xu Yi56,Zhang Tong-Tong56,Chen Su-Ning56,Zhu Hong-Hu34,Chen Zhu1ORCID,Jin Jie347,Wu De-Pei56ORCID,Shen Yang1,Chen Sai-Juan1ORCID

Affiliation:

1. Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

2. School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200025, China

3. Department of Hematology, The First Affiliated Hospital, Zhejiang University College of Medicine, Hangzhou, Zhejiang 310003, China

4. Key Laboratory of Hematologic Malignancies, Diagnosis and Treatment, Hangzhou, Zhejiang 310003, China

5. National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China

6. Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou 215006, China

7. Zhejiang University Cancer Center, Hangzhou, Zhejiang 310003, China

Abstract

The current classification of acute myeloid leukemia (AML) relies largely on genomic alterations. Robust identification of clinically and biologically relevant molecular subtypes from nongenomic high-throughput sequencing data remains challenging. We established the largest multicenter AML cohort (n = 655) in China, with all patients subjected to RNA sequencing (RNA-Seq) and 619 (94.5%) to targeted or whole-exome sequencing (TES/WES). Based on an enhanced consensus clustering, eight stable gene expression subgroups (G1–G8) with unique clinical and biological significance were identified, including two unreported (G5 and G8) and three redefined ones (G4, G6, and G7). Apart from four well-known low-risk subgroups including PML::RARA (G1), CBFB::MYH11 (G2), RUNX1::RUNX1T1 (G3), biallelic CEBPA mutations or -like (G4), four meta-subgroups with poor outcomes were recognized. The G5 (myelodysplasia-related/-like) subgroup enriched clinical, cytogenetic and genetic features mimicking secondary AML, and hotspot mutations of IKZF1 (p.N159S) (n = 7). In contrast, most NPM1 mutations and KMT2A and NUP98 fusions clustered into G6–G8, showing high expression of HOXA / B genes and diverse differentiation stages, from hematopoietic stem/progenitor cell down to monocyte, namely HOX -primitive (G7) , HOX -mixed (G8), and HOX -committed (G6). Through constructing prediction models, the eight gene expression subgroups could be reproduced in the Cancer Genome Atlas (TCGA) and Beat AML cohorts. Each subgroup was associated with distinct prognosis and drug sensitivities, supporting the clinical applicability of this transcriptome-based classification of AML. These molecular subgroups illuminate the complex molecular network of AML, which may promote systematic studies of disease pathogenesis and foster the screening of targeted agents based on omics.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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